Canonical Allele Identifier: CA2646704612

Gene: DPYD DPYD-AS1

Linked Data

• gnomAD v4: 1-97305360-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.97305361dup , CM000663.2:g.97305361dup	GRCh38
NC_000001.10:g.97770917dup , CM000663.1:g.97770917dup	GRCh37
NC_000001.9:g.97543505dup	NCBI36
NG_008807.2:g.620699dup , LRG_722:g.620699dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370192.8:c.2197dup (DPYD) MANE Select	ENSP00000359211.3:p.Thr733AsnfsTer15
ENST00000370192.7:c.2197dup (DPYD)	ENSP00000359211.3:p.Thr733AsnfsTer15
NM_000110.3:c.2197dup , LRG_722t1:c.2197dup (DPYD)	NP_000101.2:p.Thr733AsnfsTer15
NR_046590.1:n.129-828dup (DPYD-AS1)
XM_005270562.3:c.1981dup (DPYD)	XP_005270619.2:p.Thr661AsnfsTer15
XM_006710397.2:c.2197dup (DPYD)	XP_006710460.1:p.Thr733AsnfsTer15
XM_006710397.3:c.2197dup (DPYD)	XP_006710460.1:p.Thr733AsnfsTer15
XM_017000507.1:c.2086dup (DPYD)	XP_016855996.1:p.Thr696AsnfsTer15
XM_017000508.2:c.1702dup (DPYD)	XP_016855997.1:p.Thr568AsnfsTer15
XM_017000509.2:c.1702dup (DPYD)	XP_016855998.1:p.Thr568AsnfsTer15
XM_017000510.1:c.1702dup (DPYD)	XP_016855999.1:p.Thr568AsnfsTer15
NM_000110.4:c.2197dup (DPYD) MANE Select	NP_000101.2:p.Thr733AsnfsTer15